Charley's Fund - Fighting Duchenne Muscular Dystrophy
Charley's Fund accelerates the development of life-saving treatments for Duchenne muscular dystrophy and supports solutions to translate promise into results.
Language: English
Parent Project Muscular Dystrophy (PPMD) fights to end Duchenne muscular dystrophy. We accelerate research, raise our voices to impact policy, demand optimal care for every single family, and strive to ensure access to approved therapies.
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Harrison's Fund - The Duchenne Mental Health Charity and home of the Chrysalis Grant, giving potential access to private psychological and mental health support to newly diagnosed parents, patients and families living with Duchenne Muscular Dystrophy.
Angels for Isaac works to educate the public about Duchenne Muscular Dystrophy and how they can help in our fight to find a cure. We have kicked off our 2014 RZR Raffle. Purchase your ticket to help us put an END to Duchenne Muscular Dystrophy, a terminal muscle wasting disease with no treatment and no cure!
FDMD are aggressively raising money for Duchenne Muscular Dystrophy research. Our hope is to find a cure for this horrible disease.
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Families Supporting Families You are not alone. Whether you are dealing with a new diagnosis of Duchenne Muscular Dystrophy (DMD), or are further along in the journey, the Duchenne Family Support Group is here for you. Our helpline: 0800 121 4518 The DFSG is a UK national charity, run by families for families affected by
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CureDuchenne's mission - cure Duchenne muscular dystrophy (DMD). Our venture philanthropy model funds research, early diagnosis, treatment
Associació Catalana de Persones amb Malalties Neuromusculars. Atenció individual i familiar a persones amb Duchenne, Atrofia Espinal, Steinert, Charcot Marie Tooth, Miastenia,
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